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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACPD</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics Discussions</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACPD</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7375</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acpd-11-2407-2011</article-id>
<title-group>
<article-title>Estimating the influence of the secondary organic aerosols on present climate using ECHAM5-HAM</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>O&apos;Donnell</surname>
<given-names>D.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tsigaridis</surname>
<given-names>K.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Feichter</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Max Planck Institute for Meteorology, Bundesstrasse 55, 20146 Hamburg, Germany</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Laboratoire des Sciences du Climat et de l&apos;Environnement (LSCE), 91191 Gif-sur-Yvette, France</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>now at: Institute for Atmospheric Science and Climate, ETH Zürich, Universitätstrasse 16, 8092 Zürich, Switzerland</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>now at: Center for Climate System Research, Columbia University and NASA Goddard Institute for Space Studies, 2880 Broadway, New York NY10025, USA</addr-line>
</aff>
<pub-date pub-type="epub">
<day>24</day>
<month>01</month>
<year>2011</year>
</pub-date>
<volume>11</volume>
<issue>1</issue>
<fpage>2407</fpage>
<lpage>2472</lpage>
<permissions>
<license xlink:type="simple">
<license-p>This is an open-access article ditributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
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<self-uri xlink:href="http://www.atmos-chem-phys-discuss.net/11/2407/2011/acpd-11-2407-2011.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys-discuss.net/11/2407/2011/acpd-11-2407-2011.pdf</self-uri>
<abstract>
<p>In recent years, several field measurement campaigns have
      highlighted the importance of the organic fraction of aerosol
      mass, and with such spatial diversity that one may assert that
      these aerosols are ubiquitous in the troposphere, with
      particular importance in continental areas. Investigation of
      the chemical composition of organic aerosol remains a work in
      progress, but it is now clear that a significant portion of
      the total organic mass is composed of secondary organic
      material, that is, aerosol chemically formed from gaseous
      volatile organic carbon (VOC) precursors. A number of such
      precursors, of both biogenic and anthropogenic origin, have
      been identified. Experimental, inventory building and
      modelling studies have followed. Laboratory studies have
      yielded information on the chemical pathways that lead to
      secondary organic aerosol (SOA) formation, and provided the
      means to estimate the aerosol yields from a given
      precursor-oxidant reaction. Global inventories of
      anthropogenic VOC emissions, and of biogenic VOC emitter
      species distribution and their emission potential have been
      constructed. Models have been developed that provide global
      estimates of precursor VOC emissions, SOA formation and
      atmospheric burdens of these species. This paper estimates the direct and indirect effects of these aerosols using the global climate-aerosol model ECHAM5-HAM. For
      year 2000 conditions, we estimate a global annual mean
      shortwave (SW) aerosol direct effect due to SOA of
      &amp;minus;0.3 W m&lt;sup&gt;&amp;minus;2&lt;/sup&gt;. The model predicts a positive SW indirect
      effect due to SOA amounting to +0.23 W m&lt;sup&gt;&amp;minus;2&lt;/sup&gt;, arising
      from enlargement of particles due to condensation of SOA,
      together with an enhanced coagulation sink for small
      particles. Longwave effects are small. Finally, we indicate of
      areas of research into SOA that are required in order to
      better constrain our estimates of the influence of aerosols on
      the climate system.</p>
</abstract>
<counts><page-count count="66"/></counts>
</article-meta>
</front>
<body/>
<back>
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